Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Apr 2024. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5309963015 | CHD8-related intellectual disability, autism, macrocephaly, tall stature syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5309964014 | Chromodomain helicase DNA binding protein 8 overgrowth syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5309966011 | CHD8 overgrowth syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5309967019 | Chromodomain helicase DNA binding protein 8 overgrowth syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5309965010 | A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of mild to moderate intellectual disability, autism spectrum phenotype, macrocephaly, tall stature, gastrointestinal problems (including recurrent constipation), distinctive facial features (including wide-set eyes with down-slanted palpebral fissure, broad nose with full nasal tip, pointed chin and broad forehead with prominent supraorbital ridge) and sleep problems. Other clinical manifestations include anxiety problems, attention problems, impaired social interactions, and seizures. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
CHD8 overgrowth syndrome | Is a | Multiple malformation syndrome with early overgrowth | true | Inferred relationship | Some | ||
CHD8 overgrowth syndrome | Is a | Neurodevelopmental disorder | true | Inferred relationship | Some | ||
CHD8 overgrowth syndrome | Is a | Genetic disease | true | Inferred relationship | Some | ||
CHD8 overgrowth syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
CHD8 overgrowth syndrome | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
CHD8 overgrowth syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)